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Favourable Outcome in a 33-Year-Old Female with Acute Haemorrhagic Leukoencephalitis

BACKGROUND: Acute haemorrhagic leukoencephalitis (AHLE) is a rare and rapidly fatal disease of unknown aetiology. There is a paucity of literature on the presentation and management of this rare disease. CASE DESCRIPTION: We report the case of a 33-year-old female presenting with headache and left-s...

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Autores principales: Solis, Waldo G., Waller, Sophie E., Harris, Angela K., Sugo, Ella, Hansen, Mitchell A., Lechner-Scott, Jeanette
Formato: Online Artículo Texto
Lenguaje:English
Publicado: S. Karger AG 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5437433/
https://www.ncbi.nlm.nih.gov/pubmed/28559834
http://dx.doi.org/10.1159/000472706
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author Solis, Waldo G.
Waller, Sophie E.
Harris, Angela K.
Sugo, Ella
Hansen, Mitchell A.
Lechner-Scott, Jeanette
author_facet Solis, Waldo G.
Waller, Sophie E.
Harris, Angela K.
Sugo, Ella
Hansen, Mitchell A.
Lechner-Scott, Jeanette
author_sort Solis, Waldo G.
collection PubMed
description BACKGROUND: Acute haemorrhagic leukoencephalitis (AHLE) is a rare and rapidly fatal disease of unknown aetiology. There is a paucity of literature on the presentation and management of this rare disease. CASE DESCRIPTION: We report the case of a 33-year-old female presenting with headache and left-sided apraxia. Imaging revealed a right-sided white matter lesion with extensive cytotoxic oedema. Pathology was suggestive of AHLE. She underwent an open excisional biopsy and was treated with high-dose corticosteroids. Three months since symptom onset she remains clinically well with resolving apraxia and radiological appearance. CONCLUSION: This case may represent a milder spectrum of AHLE, which responded favourably to corticosteroids.
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spelling pubmed-54374332017-05-30 Favourable Outcome in a 33-Year-Old Female with Acute Haemorrhagic Leukoencephalitis Solis, Waldo G. Waller, Sophie E. Harris, Angela K. Sugo, Ella Hansen, Mitchell A. Lechner-Scott, Jeanette Case Rep Neurol Case Report BACKGROUND: Acute haemorrhagic leukoencephalitis (AHLE) is a rare and rapidly fatal disease of unknown aetiology. There is a paucity of literature on the presentation and management of this rare disease. CASE DESCRIPTION: We report the case of a 33-year-old female presenting with headache and left-sided apraxia. Imaging revealed a right-sided white matter lesion with extensive cytotoxic oedema. Pathology was suggestive of AHLE. She underwent an open excisional biopsy and was treated with high-dose corticosteroids. Three months since symptom onset she remains clinically well with resolving apraxia and radiological appearance. CONCLUSION: This case may represent a milder spectrum of AHLE, which responded favourably to corticosteroids. S. Karger AG 2017-05-05 /pmc/articles/PMC5437433/ /pubmed/28559834 http://dx.doi.org/10.1159/000472706 Text en Copyright © 2017 by S. Karger AG, Basel http://creativecommons.org/licenses/by-nc/4.0/ This article is licensed under the Creative Commons Attribution-NonCommercial-4.0 International License (CC BY-NC) (http://www.karger.com/Services/OpenAccessLicense). Usage and distribution for commercial purposes requires written permission.
spellingShingle Case Report
Solis, Waldo G.
Waller, Sophie E.
Harris, Angela K.
Sugo, Ella
Hansen, Mitchell A.
Lechner-Scott, Jeanette
Favourable Outcome in a 33-Year-Old Female with Acute Haemorrhagic Leukoencephalitis
title Favourable Outcome in a 33-Year-Old Female with Acute Haemorrhagic Leukoencephalitis
title_full Favourable Outcome in a 33-Year-Old Female with Acute Haemorrhagic Leukoencephalitis
title_fullStr Favourable Outcome in a 33-Year-Old Female with Acute Haemorrhagic Leukoencephalitis
title_full_unstemmed Favourable Outcome in a 33-Year-Old Female with Acute Haemorrhagic Leukoencephalitis
title_short Favourable Outcome in a 33-Year-Old Female with Acute Haemorrhagic Leukoencephalitis
title_sort favourable outcome in a 33-year-old female with acute haemorrhagic leukoencephalitis
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5437433/
https://www.ncbi.nlm.nih.gov/pubmed/28559834
http://dx.doi.org/10.1159/000472706
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